Brain Diseases

Displaying 1 - 10 of 10CSV
Kassabian, B., Levy, A. M., Gardella, E., Aledo‐Serrano, A., Ananth, A. L., Brea‐Fernández, A. J., Caumes, R., Chatron, N., Dainelli, A., De Wachter, M., Denommé‐Pichon, A., Dye, T. J., Fazzi, E., Felt, R., Fernández‐Jaén, A., Fernández‐Prieto, M., Gantz, E., Gasperowicz, P., Gil‐Nagel, A., … Rubboli, G. (2024). Developmental epileptic encephalopathy in DLG4‐related synaptopathy. Epilepsia, 65(4), 1029–1045. Portico. https://doi.org/10.1111/epi.17876
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Kelly, J. F., Greene, M. C., & Abry, A. (2024). America’s perceptions of opioid related impairment: A national randomized study examining how different individuals may stigmatize addiction in response to different terminology. Journal of Substance Use and Addiction Treatment, 157, 209288. https://doi.org/10.1016/j.josat.2023.209288
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Columbia Affiliation
Monfrini, E., Arienti, F., Rinchetti, P., Lotti, F., & Riboldi, G. M. (2023). Brain Calcifications: Genetic, Molecular, and Clinical Aspects. International Journal of Molecular Sciences, 24(10), 8995. https://doi.org/10.3390/ijms24108995
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Michael, B. D., Walton, D., Westenberg, E., García-Azorín, D., Singh, B., Tamborska, A. A., Netravathi, M., Chomba, M., Wood, G. K., Easton, A., Siddiqi, O. K., Jackson, T. A., Pollak, T. A., Nicholson, T. R., Nair, S., Breen, G., Prasad, K., Thakur, K. T., … Chou, S. H.-Y. (2023). Consensus Clinical Guidance for Diagnosis and Management of Adult COVID-19 Encephalopathy Patients. The Journal of Neuropsychiatry and Clinical Neurosciences, 35(1), 12–27. https://doi.org/10.1176/appi.neuropsych.22010002
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Rabadan, M. A., De La Cruz, E. D., Rao, S. B., Chen, Y., Gong, C., Crabtree, G., Xu, B., Markx, S., Gogos, J. A., Yuste, R., & Tomer, R. (2022). An in vitro model of neuronal ensembles. Nature Communications, 13(1). https://doi.org/10.1038/s41467-022-31073-1
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Ganapathi, M., Friocourt, G., Gueguen, N., Friederich, M. W., Le Gac, G., Okur, V., Loaëc, N., Ludwig, T., Ka, C., Tanji, K., Marcorelles, P., Theodorou, E., Lignelli‐Dipple, A., Voisset, C., Walker, M. A., Briere, L. C., Bourhis, A., Blondel, M., LeDuc, C., … Chung, W. K. (2022). A homozygous splice variant in ATP5PO, disrupts mitochondrial complex V function and causes Leigh syndrome in two unrelated families. Journal of Inherited Metabolic Disease, 45(5), 996–1012. Portico. https://doi.org/10.1002/jimd.12526
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